Determination of Tolbutamide in Rabbit Plasma by LC-MS/MS and Its Application to Pharmacokinetic Study

被引:0
作者
Wang, Xuebao [1 ]
Lin, Guanyang [2 ]
Hu, Lufeng [2 ]
Xu, Xuegu [3 ]
Jiang, Haiyan [3 ]
Pan, Yibin [3 ]
Wang, Xianqin [1 ]
机构
[1] Wenzhou Med Coll, Analyt & Testing Ctr, Wenzhou 325035, Peoples R China
[2] Wenzhou Med Coll, Affiliated Hosp 1, Wenzhou 325000, Peoples R China
[3] Wenzhou Med Coll, Sch Pharm, Wenzhou 325035, Peoples R China
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2010年 / 29卷 / 05期
关键词
LC-MS/MS; Plasma; Pharmacokinetics; Tolbutamide; PERFORMANCE LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; URINE; HYDROXYLATION; METABOLITES; INHIBITION; OXIDATION; DRUGS; SERUM;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A sensitive and selective liquid chromatography tandem mass spectrometry method (LC-MS/MS) for the determination of tolbutamide in rabbit plasma was developed and validated over the concentration range of 4-1000 ng mL(-1). After addition of bupivacaine as internal standard (IS), a simplified protein precipitation with acetonitrile was employed for the sample preparation. Chromatographic separation was performed by an Agilent Zorbax SB-C18 column (150 mm?2.1 mm, 3.5 mu m). The mobile phase was acetonitrile-1% formic acid in water (50:50 v/v) delivered at a flow rate of 0.3 mL mm(-1). The MS data acquisition was accomplished by multiple reactions monitoring (MRM) mode with positive electrospray ionization (ESI) interface. The lower limit of quantification (LLOQ) was 4 ng mL(-1). For interday and intra-day tests, the precision (RSD) for the entire validation was less than 10%, and the accuracy was within the 94.7% to 105.6% range. The validated method is successfully used to analyze the drug in samples of rabbit plasma for pharmacokinetic study.
引用
收藏
页码:789 / 794
页数:6
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